Senior Specialist- Regulatory Science

Senior Regulatory Affairs Specialist

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere.

Job Description

The Senior Regulatory Affairs Specialist supports US regulatory activities for Animal Health pharmaceutical and biological products. The role provides hands-on support across product labeling, regulatory operations, lifecycle management, regulatory submissions, product stewardship, and compliance activities. The position works closely with internal and client stakeholders to ensure regulatory activities are completed accurately, compliantly, and within required timelines.

Responsibilities:

• Support US labeling activities for Animal Health pharmaceutical and biological products.
• Coordinate labeling development, review, approval, implementation, and maintenance.
• Prepare and coordinate regulatory submissions, registrations, annual reports, and postapproval changes.
• Support regulatory operations, document workflows, submission tracking, and records management.
• Maintain regulatory documentation, correspondence, trackers, and product information.
• Support lifecycle management and product stewardship activities.
• Evaluate product, labeling, manufacturing, and quality changes for potential regulatory impact.
• Collaborate with Regulatory Affairs, Quality, Manufacturing, Pharmacovigilance, Supply Chain, and Commercial teams.
• Support onboarding, training, knowledge transfer, and regulatory-system activities.
• Ensure assigned deliverables comply with applicable procedures and regulatory requirements.
• Manage multiple priorities and communicate potential risks or delays promptly.
• Support other US regulatory consulting activities as business needs evolve.

Education

• Bachelor's degree in a scientific, regulatory, pharmaceutical, or related discipline.
• Certification in clinical research or regulatory affairs preferred. Certification in data analytics or scientific data interpretation tools preferred.

Experience

• Five or more years of regulatory affairs, regulatory operations, labeling, pharmaceutical, biologics, vaccines, or related experience.
• Experience supporting regulatory submissions, labeling, lifecycle management, or regulatory operations.
• Experience working with cross-functional teams in a regulated environment.

Skills

• Strong documentation, organization, communication, and problem-solving skills.
• Ability to manage multiple assignments and work independently.